PPM - Neurofibromatosis Type 2 (NF2)-Checklist

Checklist

Pdf Summary

This document is a checklist for healthcare professionals to use during patient visits for Neurofibromatosis Type 2 (NF2). It includes various elements that should be reviewed and documented, such as the diagnosis and diagnostic criteria, family history, vital signs, and subjective reports of symptoms. The checklist also emphasizes the importance of conducting a hearing evaluation and high resolution head MRI, as well as potential referrals to other specialists. Genetic testing is discussed, along with the need for pre-test counseling and the possibility of multiple testing methods. The results of genetic testing and any identified tissue samples should be documented. Additionally, post-test counseling, reproductive options, and the identification of at-risk family members should be addressed and documented. The document also suggests discussing resources for support and therapeutic options with patients. Lastly, it advises continuing follow-up or considering genetic testing for patients under 30 who do not meet clinical criteria for NF2.

Keywords

checklist

Neurofibromatosis Type 2

diagnosis

family history

genetic testing

hearing evaluation

MRI

referrals

counseling

support